Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4821481
MYH9
1.000 0.080 22 36299896 intron variant C/T snv 0.78 1
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs538166970
ACE
0.925 0.080 17 63496920 missense variant G/A;C snv 1.6E-05; 4.0E-06 2
rs61747728
NPHS2
0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 7
rs754919065
TRPC6
1.000 0.080 11 101504767 missense variant G/A snv 6.1E-05; 4.1E-06 7.0E-06 1
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77 9
rs760336723
PODXL
0.882 0.240 7 131506292 missense variant G/A snv 2.8E-05 5.6E-05 3
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4